Drug intelligence / Profile preview

emylcamate

Development stage
Discontinued
Lead developer
Merck
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Reversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules, Allosteric Modulators → Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

Emylcamate is a small molecule anxiolytic and muscle relaxant of the carbamate ester class. It was developed and marketed in the early 1960s under the brand name Striatran by Merck for the treatment of anxiety and tension[1][6][7]. Emylcamate acts primarily as a central nervous system depressant by enhancing GABAergic activity; specifically, it is a positive allosteric modulator at Gamma-aminobutyric acid receptor subunit alpha (GABA-A receptor), increasing inhibitory neurotransmission to produce sedative and anxiolytic effects[5]. Preclinical studies indicated that emylcamate had greater potency and faster onset than meprobamate, but it was eventually replaced by meprobamate in clinical use[1][6]. The drug is no longer prescribed.

Brand names
Striatran
Other names
3-methylpentan-3-yl carbamate3-methyl-3-pentanol carbamateEmilcamatoEmylcamat
02

Targets

GABRR (GABA-A receptor subunit rho)

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